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. Author manuscript; available in PMC: 2019 Nov 4.
Published in final edited form as: Indoor Air. 2018 May 4:10.1111/ina.12470. doi: 10.1111/ina.12470

Table 4.

Agreement in identification of common genus between DNA sequencing and culture method in 22 dust samples

Genus* Kappa
statistics**
Total detection
% (no. of samples)
% of
common
detection
% of exclusive
detection
DNA Culture DNA Culture
Alternaria −0.08 27.3 (6) 4.6 (1) 0 27.3 4.6
Aspergillus 0.27 50 (11) 77.3 (17) 45.5 4.6 31.8
Aureobasidium 0 72.7 (16) 50 (11) 36.4 36.4 13.6
Botrytis −0.08 18.2 (4) 4.6 (1) 0 18.2 4.6
Chaetomium −0.08 4.6 (1) 27.3 (6) 0 4.6 27.3
Cladosporium 0.07 18.2 (4) 86.4 (19) 18.2 0 68.2
Epicoccum 0.14 54.6 (12) 77.3 (17) 45.5 9.1 31.8
Fusarium −0.12 13.6 (3) 9.1 (2) 0 13.6 9.1
Mucor −0.09 40.9 (9) 27.3 (6) 9.1 31.8 18.2
Penicillium§ 36.4 (8) 100 (22) 36.4 0 63.6
Phoma −0.06 22.7 (5) 68.2 (15) 13.6 9.1 54.6
Pithomyces 0.11 72.7 (16) 13.6 (3) 13.6 59.1 0
*

Genus which was detected in more than 20% of samples by either culture or DNA sequencing method was only included in this analysis.

**

Kappa score: no agreement (<0); slight agreement (0.01–0.20); fair agreement (0.21–0.40); moderate agreement (0.41–0.60); substantial agreement (0.61–0.80); almost perfect agreement (0.81–0.99)1.

§

All samples were positive from culture method. Therefore, Kappa score could not be calculated.